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Publikováno v:
Revista médica de Chile, Volume: 140, Issue: 2, Pages: 161-168, Published: FEB 2012
Background: The identification of clinical and pathological forms of Creutzfeldt Jakob Disease (CJD) started with the first cases of the disease. Genetic and biomolecular prion status assessment are allowing now a better classification. Aim: To ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______614::131a129a1fe74d00c29bfa9b155d31aa
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872012000200003&lng=en&tlng=en
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872012000200003&lng=en&tlng=en